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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 10067Generated: October 26, 2026

Potassium Carbonate → methyl 4'-{(1R)-1-[(tert-butoxycarbonyl)amino]ethyl)-3-fluoro-1,1'-biphenyl-2-carboxylate

https://huagongshe.com/reaction/10067

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantTri-o-tolylphosphineHCID 80271—
ReactantMethyl 2-fluoro-6-iodobenzoateHCID 12192164—
Reactanttert-Butyl (R)-(1-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)ethyl)carbamateHCID 67467206—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Productmethyl 4'-{(1R)-1-[(tert-butoxycarbonyl)amino]ethyl)-3-fluoro-1,1'-biphenyl-2-carboxylateHCID 6851901418.9%

Reaction Steps

To a stirred solution of tert-butyl (1R)-1-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]ethylcarbamate (1.0 g, 2.9 mmol) and methyl 2-fluoro-6-iodobenzoate (1.2 g, 4.32 mmol) in 25 mL of a 5:1 THF:water mixture was added potassium carbonate (1.2 g, 8.64 mmol), tri-o-tolylphosphine (350 mg, 1.15 mmol) and lastly palladium acetate (65 mg, 0.29 mmol). The reaction vessel was then sealed and placed into a 90° C. oil bath for overnight stirring and heating. After about 18 hours the reaction mixture was cooled to ambient temperature and then diluted with EtOAc. The organics were washed with brine (×4), dried over sodium sulfate, filtered, and concentrated under reduced pressure to give an oil. This oil was subject to silica gel chromatography eluting with 10–60% EtOAc in hexanes to provide methyl 4′-{(1R)-1-[(tert-butoxycarbonyl)amino]ethyl}-3-fluoro-1,1′-biphenyl-2-carboxylate (205 mg), found to be pure by LC/MS and proton NMR.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07091380B2
Source datasetuspto-grants-2006_08
ORD IDord-64b4a14edf7a46439a5c7511642b0ba2
Source noteuspto-grants-2006_08